Fibrodysplasia ossificans progressiva: A case report

Authors

  • Sreedhar Vasala Mamata Medical College
  • V Dharma Rao Mamata Medical College
  • M Rajaneesh Reddy Mamata Medical College
  • P Ramyatha Reddy Mamata Medical College
  • K Murali Mamata Medical College

DOI:

https://doi.org/10.3126/ajms.v5i4.9915

Keywords:

Myositis ossificans progressiva, Genetic disorder, Autosomal dominant, Ossifications

Abstract

Fibrodysplasia ossificans progressiva (FOP) is a genetic disorder with unknown cause. Disease is characterized by heterotopic ossifications of connective tissue and congenital malformations of distal part of extremities. Most cases are sporadic and transmitted as autosomal dominant. As very few cases of FOP are being reported in Indian literature, we, therefore, report one such case here.

Our case is a 20 years-old female patient who had bilateral short great toes with hallux valgus associated with heterotopic ossifications of connective tissue with restrictions of range of motion and disability of daily living activities. We have diagnosed it as FOP based on our physical examination and skeletal x-rays findings.

DOI: http://dx.doi.org/10.3126/ajms.v5i4.9915

Asian Journal of Medical Sciences 2014 Vol.5(4); 113-115

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Author Biographies

Sreedhar Vasala, Mamata Medical College

Assistant Professor, Department of General Medicine

V Dharma Rao, Mamata Medical College

Professor, Department of General/Internal Medicine

M Rajaneesh Reddy, Mamata Medical College

Assistant Professor, Department of General Medicine

P Ramyatha Reddy, Mamata Medical College

PG Resident, Department of General Medicine

K Murali, Mamata Medical College

PG Resident, Department of General Medicine

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Published

2014-05-17

How to Cite

Vasala, S., Rao, V. D., Reddy, M. R., Reddy, P. R., & Murali, K. (2014). Fibrodysplasia ossificans progressiva: A case report. Asian Journal of Medical Sciences, 5(4), 113–115. https://doi.org/10.3126/ajms.v5i4.9915

Issue

Vol. 5 No. 4 (2014)

Section

Case Reports

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